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The use of smart watch technology to improve the management of patients presenting with fast irregular heart rates in the Emergency department - a pilot study

Use of single lead ECG to assist cardioversion in atrial fibrillation in the Emergency department - a pilot study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12620001374954
Acronym
SELECTED
Enrollment
26
Registered
2020-12-22
Start date
2021-02-08
Completion date
2021-12-31
Last updated
2025-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The use of smart watch technology to improve the management of patients presenting with fast irregular heart rates (AF) in the Emergency department (ED). Participants will be given a Alivecor single lead ECG device to monitor their heart rhythm every 6 hours for the next 48 hours. If after 48 hours the heart rhythm has reverted to normal no further visits to ED are required. If they remain in AF they will return to the ED for an elective cardioversion to restore a normal heart rhythm. The aim of the study to the improve the management of these patients in ED and reduce the number of visits to ED.

Interventions

Recruit 50 participants (Intervention group) with atrial fibrillation (AF) where the onset is less than 24 hours before presentation to emergency department (ED), who are able to have delayed cardioversion in addition to standard medical care. These participants will receive at home monitoring of their heart rhythm with the Alivecor mobile single lead electrocardiogram (ECG) device. The participants will be required to record and transmit each single lead ECG every 6 hours for 48 hours. Particip

Recruit 50 participants (Intervention group) with atrial fibrillation (AF) where the onset is less than 24 hours before presentation to emergency department (ED), who are able to have delayed cardioversion in addition to standard medical care. These participants will receive at home monitoring of their heart rhythm with the Alivecor mobile single lead electrocardiogram (ECG) device. The participants will be required to record and transmit each single lead ECG every 6 hours for 48 hours. Participants will receive a text message and/ or phone call if a ECG recording is missing. If normal rhythm is restored spontaneously within 48 hours, they will not be required to return to ED. The minority (31%) of participants with ongoing AF will be instructed to return to ED for a scheduled cardioversion. In both scenarios, after the initial 48 hour period, the patient will be asked to record and send ECGs twice weekly, which will be reviewed by the research team. Four weeks later, they will have a follow-up cardiology appointment, either in person or via telemedicine.

Sponsors

Eastern Health
Lead SponsorHospital

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Diagnosis
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

50 patients with AF onset less than 24 hours presenting to ED who are able to have delayed cardioversion. • Age: 18 years or greater • Residing within the Eastern Health catchment during the initial intervention period (48 hours from time of ED presentation) • Haemodynamically stable • Recent onset AF : <24 hours of symptomatic first episode or recurrent AF • Have compatible smart phone or tablet to use the Alivecor device

Exclusion criteria

• AF onset time unclear. • History of long-standing persistent AF (continuous AF for more than 1 year) • Patients with haemodynamically unstable AF who require emergent cardioversion • Have a cardiac pacemaker or implantable cardioverter defribrillator or other implanted electronic device • Unable to provide informed consent

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026